Department of Dermatology, Gangnam Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Dermatology, Gangnam Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
J Dermatol Sci. 2020 Apr;98(1):41-49. doi: 10.1016/j.jdermsci.2020.02.006. Epub 2020 Feb 21.
Endoplasmic reticulum (ER) calcium depletion-induced ER stress is a crucial signal for keratinocyte differentiation and barrier homeostasis, but its effects on the epidermal tight junction (TJ) have not been characterized. Ultraviolet B (UVB) causes ER calcium release in keratinocytes and disrupts epidermal TJ, however, the involvement of ER stress in the UVB-induced TJ alterations remains unknown.
To investigate the effect of ER stress by pharmacological ER calcium depletion or UVB on the TJ integrity in normal human epidermal keratinocytes (NHEK).
NHEK were exposed to ER calcium pump inhibitor thapsigargin (Tg) or UVB. ER stress markers and TJ molecules expression, TJ and F-actin structures, and TJ barrier function were analyzed.
Tg or UVB exposure dose-dependently triggered unfolded protein response (UPR) in NHEK. Low dose Tg induced the IRE1α-XBP1 pathway and strengthened TJ barrier. Contrary, high dose Tg activated PERK phosphorylation and disrupted TJ by F-actin disorganization. UVB disrupted TJ and F-actin structures dose dependently. IRE1α RNase inhibition induced or exacerbated TJ and F-actin disruption in the presence of low dose Tg or UVB. High dose Tg increased RhoA activity. 4-PBA or Rho kinase (ROCK) inhibitor partially prevented the disruption of TJ and F-actin following high dose Tg or UVB.
ER stress has bimodal effects on the epidermal TJ depending on its intensity. The IRE1α pathway is critical for the maintenance of TJ integrity during mild ER stress. Severe ER stress-induced UPR or ROCK signalling mediates the disruption of TJ through cytoskeletal disorganization during severe ER stress.
内质网(ER)钙耗竭诱导的 ER 应激是角质形成细胞分化和屏障稳态的关键信号,但它对表皮紧密连接(TJ)的影响尚未确定。紫外线 B(UVB)可导致角质形成细胞 ER 钙释放并破坏表皮 TJ,但 ER 应激是否参与 UVB 诱导的 TJ 改变尚不清楚。
通过药理学 ER 钙耗竭或 UVB 研究 ER 应激对正常人体表皮角质形成细胞(NHEK)TJ 完整性的影响。
用 ER 钙泵抑制剂 thapsigargin(Tg)或 UVB 处理 NHEK。分析 ER 应激标志物和 TJ 分子的表达、TJ 和 F-肌动蛋白结构以及 TJ 屏障功能。
Tg 或 UVB 暴露剂量依赖性地触发 NHEK 未折叠蛋白反应(UPR)。低剂量 Tg 诱导 IRE1α-XBP1 通路并增强 TJ 屏障。相反,高剂量 Tg 激活 PERK 磷酸化并通过 F-肌动蛋白解聚破坏 TJ。UVB 剂量依赖性地破坏 TJ 和 F-肌动蛋白结构。在低剂量 Tg 或 UVB 存在的情况下,IRE1α RNase 抑制诱导或加剧 TJ 和 F-肌动蛋白的破坏。高剂量 Tg 增加 RhoA 活性。4-PBA 或 Rho 激酶(ROCK)抑制剂部分阻止了高剂量 Tg 或 UVB 后 TJ 和 F-肌动蛋白的破坏。
ER 应激对表皮 TJ 具有双重影响,取决于其强度。IRE1α 通路在轻度 ER 应激时对 TJ 完整性的维持至关重要。严重的 ER 应激诱导的 UPR 或 ROCK 信号通过严重的 ER 应激时细胞骨架的解聚介导 TJ 的破坏。